Abstract
Blockade of Kv1.3 K+ channels in T cells is a promising therapeutic approach for the treatment of autoimmune diseases such as multiple sclerosis and type 1 diabetes mellitus. Vm24 (α-KTx 23.1) is a novel 36-residue Kv1.3-specific peptide isolated from the venom of the scorpion Vaejovis mexicanus smithi. Vm24 inhibits Kv1.3 channels of human lymphocytes with high affinity (Kd = 2.9 pM) and exhibits >1500-fold selectivity over other ion channels assayed. It inhibits the proliferation and Ca2+ signaling of human T cells in vitro and reduces delayed-type hypersensitivity reactions in rats in vivo. Our results indicate that Vm24 has exceptional pharmacological properties that make it an excellent candidate for treatment of certain autoimmune diseases. Copyright © 2012 The American Society for Pharmacology and Experimental Therapeutics.
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CITATION STYLE
Varga, Z., Gurrola-Briones, G., Papp, F., Rodriguez De La Vega, R. C., Pedraza-Alva, G., Tajhya, R. B., … Panyi, G. (2012). Vm24, a natural immunosuppressive peptide, potently and selectively blocks Kv1.3 potassium channels of human T cells. Molecular Pharmacology, 82(3), 372–382. https://doi.org/10.1124/mol.112.078006
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